PHARMAFull-time
Safety Physician (MBBS) | Pharmacovigilance Medical Review | Immediate Joiners Preferred
DELHI NCR (IN)HYBRIDPOSTED: 9/28/2026
PHARMAFull-time
HIRING ORGANIZATIONSYNEOS HEALTHBiopharmaceutical / Healthcare Services
ROLE OVERVIEW
Perform medical review and interpretation of adverse-event and aggregate safety information for investigational and marketed products, ensuring pharmacovigilance, regulatory, SOP, and project-specific compliance.
ROLE DEFINITION & RESPONSIBILITIES
- •Perform medical review of adverse events for investigational and marketed products
- •Apply MedDRA, WHO-DRL, and safety-database knowledge including ARGUS
- •Collaborate with Safety and Pharmacovigilance colleagues on medical interpretation and case assessment
- •Ensure regulatory and SOP compliance for safety evaluation, reporting, and surveillance
- •Identify, communicate, and manage potential safety issues
- •Provide medical review and interpretation of aggregate safety reports including annual safety reports, PSURs, and PADERs
- •Interact with client safety and medical personnel
- •Mentor and train internal safety staff including case-processing personnel
Reporting Hierarchy: Reports within the Safety/Pharmacovigilance organization and collaborates with client safety and medical personnel, case-processing teams, and other Clinical Solutions stakeholders
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- MBBS or equivalent medical qualification
- Pharmacovigilance medical-review experience or relevant safety experience
- Knowledge of MedDRA and WHO-DRL
- Familiarity with safety databases such as ARGUS
- Understanding of regulatory and SOP requirements for clinical and post-marketing safety
- Ability to interpret adverse-event and aggregate safety information
PREFERRED QUALIFICATIONS
- •Experience with aggregate safety reports such as PSURs and PADERs
- •Experience supporting investigational and marketed products
- •Experience mentoring safety or case-processing staff
- •Relevant clinical or drug-development experience
- •Immediate availability to join
REQUIRED VERIFIED SKILLS
Pharmacovigilance
medical review
adverse-event assessment
MedDRA
WHO-DRL
ARGUS
safety databases
aggregate safety reports
PSUR
PADER
regulatory compliance
SOP compliance
clinical safety
post-marketing safety
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Career development and progression; supportive line management; technical and therapeutic-area training; peer recognition; total rewards program; inclusive work environment.
The supplied posting does not disclose salary, bonus, or equity. Compensation should be confirmed directly with Syneos Health; no figures have been inferred.
ORGANIZATION CONTEXT & CULTURE
Syneos Health is a global life sciences services organization providing integrated services across drug development and commercialization. Its Clinical Solutions teams support pharmaceutical and healthcare customers across clinical and safety programs.
TEAM SIZE: 25,000+ employees
INDUSTRY: Biopharmaceutical / Healthcare Services
Culture: Syneos Health describes its culture as collaborative, agile, inclusive, development-focused, and driven by delivering solutions that support healthcare and patient progress.
EXPECTED CAREER ROADMAP
Potential progression into senior Safety Physician, Pharmacovigilance Medical Reviewer, safety leadership, signal-management, aggregate-reporting, or broader drug-safety medical roles depending on experience and organizational opportunities.
APPLICATION ADVISORY
Emphasize the MBBS qualification and pharmacovigilance medical-review experience; highlight adverse-event assessment, MedDRA, ARGUS, PSUR/PADER review, regulatory compliance, and safety surveillance; demonstrate experience working with safety and medical stakeholders; mention immediate availability if applicable.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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